Exercise training-induced PPARβ increases PGC-1α protein stability and improves insulin-induced glucose uptake in rodent muscles

JS Park, JO Holloszy, K Kim, JH Koh - Nutrients, 2020 - mdpi.com
JS Park, JO Holloszy, K Kim, JH Koh
Nutrients, 2020mdpi.com
This study aimed to investigate the long-term effects of training intervention and resting on
protein expression and stability of peroxisome proliferator-activated receptor β/δ (PPARβ),
peroxisome proliferator-activated receptor gamma coactivator 1-α (PGC1α), glucose
transporter type 4 (GLUT4), and mitochondrial proteins, and determine whether glucose
homeostasis can be regulated through stable expression of these proteins after training.
Rats swam daily for 3, 6, 9, 14, or 28 days, and then allowed to rest for 5 days post-training …
This study aimed to investigate the long-term effects of training intervention and resting on protein expression and stability of peroxisome proliferator-activated receptor β/δ (PPARβ), peroxisome proliferator-activated receptor gamma coactivator 1-α (PGC1α), glucose transporter type 4 (GLUT4), and mitochondrial proteins, and determine whether glucose homeostasis can be regulated through stable expression of these proteins after training. Rats swam daily for 3, 6, 9, 14, or 28 days, and then allowed to rest for 5 days post-training. Protein and mRNA levels were measured in the skeletal muscles of these rats. PPARβ was overexpressed and knocked down in myotubes in the skeletal muscle to investigate the effects of swimming training on various signaling cascades of PGC-1α transcription, insulin signaling, and glucose uptake. Exercise training (Ext) upregulated PPARβ, PGC-1α, GLUT4, and mitochondrial enzymes, including NADH-ubiquinone oxidoreductase (NUO), cytochrome c oxidase subunit I (COX1), citrate synthase (CS), and cytochrome c (Cyto C) in a time-dependent manner and promoted the protein stability of PPARβ, PGC-1α, GLUT4, NUO, CS, and Cyto C, such that they were significantly upregulated 5 days after training cessation. PPARβ overexpression increased the PGC-1α protein levels post-translation and improved insulin-induced signaling responsiveness and glucose uptake. The present results indicate that Ext promotes the protein stability of key mitochondria enzymes GLUT4, PGC-1α, and PPARβ even after Ext cessation.
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